Replacement of the disulfide bond in oxytocin by an amide group

Jan 1, 1978 - Replacement of the disulfide bond in oxytocin by an amide group. Synthesis and some biological properties of [cyclo-(1-L-aspartic acid, ...
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Journal o f Medicinal Chemistry, 1978, Vol. 21, No. 1 117

Notes (10) P. Holton, Br. J . Pharmacol. Chemother., 3, 328 (1948); R. A. Munsick, Endocrinology, 66, 451 (1960). (11) J. M. Coon, Arch. Int. Pharmacodyn. Ther., 62,79 (1939); “The Pharmacopeia of the United States of America”, 18th revision, Mack Publishing Co., Easton, Pa., 1970, p 469; R. A. Munsick, W. H. Sawyer, and H. B. van Dyke, Endocrinology, 66, 860 (1960). (12) “The Pharmacopeia of the United States of America”, 18th revision, Mack Publishing Co., Easton, Pa., 1970, p 771. (13) W. A. Jeffers, M. M. Livezey, and J. H. Austin, Proc. SOC. Exp. Biol. Med., 50, 184 (1942); W. H. Sawyer, Endocrinology, 63, 694 (1958). (14) R. J. Vavrek, M. F. Ferger, G. A. Allen, D. H. Rich, A. T. Blomquist, and V. du Vigneaud, J . Med. Chem., 15, 123 (1972). (15) pA2 values [H. 0. Schild, Br. J . Pharmacol. Chemother., 2,189 (1947)] represent the negative logarithm to the base

10 of the average molar concentration of an antagonist which will reduce the response t o 2x units of pharmacologically active compound (agonist) to the response to x units of agonist. Eight individual determinations on three animals were performed and the results are given as the mean f the

standard deviation. For details of the experimental method, see Vavrek et al.’* (16) W. Y. Chan and N. Kelley, J . Pharmacol. Exp. Ther., 156, 150 (1967). (17) C. W. Smith, S. Chan, and R. Walter, J. Pharmacol. Exp.

Ther., in press. (18) R. Walter, I. L. Schwartz, J. H. Darnell, and D. W. Urry, Proc. Natl. Acad. Sci. U.S.A., 68, 1355 (1971). (19) R. Walter, Fed. Proc., Fed. Am. SOC.Exp. Biol., 36, 1872 (1977). (20) C. W. Smith, M. F. Ferger, and W. Y. Chan, J. Med. Chem., 18, 822 (1975). (21) E. Kaiser, R. L. Colescott, C. D. Bossinger, and P. I. Cook, Anal. Biochem., 34,595 (1970); D. F. Dyckes, J. J. Nestor, Jr., M. F. Ferger, and V. du Vigneaud, J . Med. Chem., 17, 250 (1974). (22) G. L. Ellman, Arch. Biochem. Biophys., 193, 265 (1951). (23) 0. H. Lowry, N. J. Rosebrough, A. L. Farr, and R. J. Randall, J . Biol. Chem., 193, 265 (1951). (24) D. H. Spackman,W. H. Stein, and S. Moore, Anal. Chem., 30, 1190 (1958). (25) S . Moore, J . Biol. Chem., 238, 235 (1963).

Replacement of the Disulfide Bond in Oxytocin by an Amide Group. Synthesis and Some Biological Properties of [ cyclo-(1-L-Aspartic acid,6-~-a,P-diaminopropionic acid)]oxytocin’ Clark W. Smith, Roderich Walter,* Department of Physiology and Biophysics, University of Illinois at the Medical Center, Chicago, Illinois 60612

Stanley Moore, Raymond C. Makofske, and Johannes Meienhofer* Chemical Research Department, Hoffmann-La Roche Incorporated, Nutley, New Jersey 07110. Received August 4, 1977

As part of a continuing investigation of the steric and electronic functions of the disulfide group in neurohypophyseal hormones on their biological activity, the synthesis of “oxytocin lactam”, [cyclo-(1-aspartic acid,6-c~,P-diaminopropionic acid)]oxytocin,has been undertaken. The protected nonapeptide was prepared in a stepwise manner by solution techniques; after removal of side-chain protecting groups, formation of the bridging amide bonds was accomplished by oxidation-reduction condensation. The analogue possesses rat uterotonic, avian vasodepressor, and rat antidiuretic potencies of 16 h 2, 6.6 h 0.6, and 5.6 h 3.8 units/mg, respectively. The disulfide bridge present in the 20-membered ring portion of neurohypophyseal hormones carries a primary responsibility for the determination of the preferred conformation of the peptide backbone2 and thereby for the topography of the peptides recognized by the various receptors responsive to these hormones. This point is dramatically illustrated by the nearly total lack of biological activity observed for the acyclic analogues, [Ala’*6]oxytocin,3 [Ala’,6]arginine-vasopressin,4and [Ser1~6]oxytocin.3The fact that the reactivity of the disulfide is not required for biological activity is amply demonstrated by the significant biological activities possessed by oxytocin analogues in which the 20-membered ring has been preserved, but one sulfur atom replaced by a methylene group&ll or both sulfur atoms by an ethylene gr0up.~9~9’~-’~ Changes of the dihedral angle of the bridging group exercise such a profound influence on the overall conformational integrity of the molecule that even a minor modification such as substitution of either one or both sulfur atoms by selenium evokes a definite change in the spectrum of biological activities.16-18 A displacement of the disulfide bond within the four-atom bridge as in [Imercaptoacetic acid,6-homocysteine]o x y t ~ c i n also ’ ~ dramatically alters the activities. In an earlier investigation of the steric and electronic functions of the disulfide group on biological activity, an

analogue of deamino-oxytocin, [cyclo-(1-@-alanine,6-aspartic acid)]oxytocin, in which the disulfide has been replaced by an amide group was synthesized.20 As an extension of this work we wish to report the synthesis and some pharmacological properties of “oxytocin lactam”, [cyclo-(1-aspartic acid,6-a,@-diaminopropionicacid)]oxytocin, (Figure 1)in which the amide group is in reverse direction of acylation as that in the previously reported “deamino-oxytocin lactam”.20~21 The synthetic route followed is summarized in Scheme I. In brief, the COOH-terminal tripeptide amide was extended in a stepwise manner using N”-benzoxycarbonyl (Z) protected amino acids coupled with dicyclohexylcarbodiimide (DCC) mediated by l-hydroxybenzotriazoleZ2 (HOBt) except for the NHz-terminal aspartic acid residue which was coupled as the N-hydroxysuccinimide active ester. In all cases catalytic hydrogenation was used to remove the Z group. The side chains of the tyrosine and aspartic acid residues were protected by the tert-butyl group and the @-amino function of the a,@-diaminopropionic acid residue was protected by the tert-butyloxycarbonyl (Boc) group. These groups were removed from the linear nonapeptide by treatment with CF3COOH and cyclization was accomplished by oxidation-reduction c o n d e n s a t i ~ n .The ~ ~ analogue was purified by gel filtration and partition chromatographyz4on Sephadex G-25.

0022-2623/78/1821-Ol17$01.00/00 1978 American Chemical Society

118 Journal of Medicinal Chemistry, 1978, Vol. 21, No. 1 CeH40H

z

o

I

CzH5

I CH2 0 I /I

1,

2

x Y t

I1

L

31

C=O

Boc

0 NH

0 6

Scheme I. Synthetic Pathway for the Preparation of [cyclo-(Asp',Dpr6)]oxytocina HC1. H-Pro-Leu-Gly-NH,

I CH-CH3 I

CH2-CH-C-NH-CH-C-NH-CH

Notes

11

5

41

CHZ-CH-NH-C-CH-NH-C-CH-(CHZ)~-CONH~

I

CHz-N \

1

I

/

CHp-CH2

I I

9

I

CHz

DCC-HOBt

Z-Asn-Dpr-Pro-Leu-Gly-NH,( 2 )

L

CH(CH3)z F i g u r e 1. General structure of the oxytocin lactam analogues, acid)]oxytocin (X [cyclo-(1-aspartic acid,6-a,P-diaminopropionic = CO; Y = NH; Z = NH2) and [cyclo-(l-/3-alanine,6-aspartic acid)]oxytocin (X = NH; Y = CO; Z = H) (reported in ref 20). Numbers indicate position of amino acid residues.

a. H,-Pd b. Z-Gln-OH, DCC-HOBt

Boc

Z-Gln-Asn-Dpr-Pro-Leu-Gly-NH, ( 3 )

1

a. H,-Pd b. Z-Ile-OH,

Boc I

DCC-HOBt

Z-Ile-Gln-Asn-Dpr-Pro-Leu-Gly-NH, (4)

But I

L

a. H,-Pd b. Z-Tyr(But)-OH,

DCC-HOBt

Boc l

Z-Tyr-Ile-Gln-Asn-Dpr-Pro-Leu-Gly-NH, ( 5)

1

a. H,-Pd b. Z-ASP(OBU~)-OSU

But I

Boc I

Z-Asp-Tyr-Ile-Gln-Asn-Dpr-Pro-Leu-Gly-NH, (6)

I

a. CF,COOH b. Mukaiyama m e t h o d

Experimental Section Details on materials and experimental methods have been described p r e v i o u ~ l y . ~Solvent ~ systems for thin-layer chromatography (Merck silica gel 60) were A, sec-BuOH-HCOOHH 2 0 (75:13.5:11.5); B, sec-BuOH-10% NHIOH (85:15); C, CHC13-MeOH (5:1). Rat uterine assays were performed on isolated horns from virgin rats in natural estrus according to the method of Holton, as modified by Munsick, with the use of Mg2+-free van DykeHastings solution as bathing Avian vasodepressor assays were performed on conscious chickens by the method of Coon, as described in the U.S. Pharmacopeia, as modified by Munsick et al.%Pressor assays were carried out on anesthetized male rats as described in the US. Pharmacopeia.n Antidiuretic assays were performed on anesthetized male rats according to the method of Jeffers et a1.,28as modified by Sawyer.29 The four-point assay design of Schildmwas used to obtain specific activities as compared to U.S.P. posterior pituitary reference standard. Z-Dpr(Boc)-Pro-Leu-Gly-NH, (1). Na-Benzyloxycarbonyl-N8-tert-butyloxycarbonyl-L-a,P-diaminopropionic acid32(3.56 g, 10.5 mmol) was dissolved in DMF (20 mL), and a solution of HC~.H-P~~-L~U-G (3.36 ~ ~g,- 10.5 N Hmmol) ~ ~ ~ in ~ DMF (20 mL) was added. The solution was cooled to 0 "C, and HOBt (2.56 g, 16.7 mmol) and DCC were added (2.4 g, 11.6 mmol), followed by NEt3 (1.47 mL, 10.5 mmol). The reaction was stirred for 45 min a t 0 "C and for 15 h a t 25 "C. Dicyclohexylurea was removed by filtration and the product precipitated by pouring the filtrate into H20. This aqueous suspension was extracted with EtOAc (3 X 100 mL). The combined organic phases were washed with 1 M citric acid (three times), HzO, 1 M NaHC03 (three times), and saline (twice), dried, and evaporated to a white residue which was crystallized from EtOAepetroleum ether: yield 4.1 g (64.6%);

a. H,-Pd b. Z-Am-OH,

Boc

CONHz

Oxytocin lactam was tested for some of the biological activities characteristic of neurohypophyseal hormones.25m The analogue possesses rat uterotonic, avian vasodepressor, and rat antidiuretic potencies of 16 f 2,6.6 f 0.6, and 5.6 f 3.8 units/mg, respectively, as compared to oxytocin with 540, 500, and 3 unitslmg, respectively. It exhibits a very weak rat pressor response which is not parallel to the response of the standard, and no estimation of its specific activity could be made. The previously reported deamino-oxytocin lactam, [cyclo-(l-/3-alanine,6-aspartic a c i d ) ] o x y t ~ c i nexhibited ,~~ milk-ejecting and uterotonic potencies of 2.93 f 0.08 and 1.13 f 0.04 units/mg, and was a weak inhibitor of the oxytocin-induced vasodepressor response. These data demonstrate that the substitution of the disulfide bond with an amide of either of the two isomeric forms results in analogues which retain sufficient conformational integrity to interact with receptors responsive to neurohypophyseal hormones.

v

Z-Dpr-Pro-Leu-Gly-NH, (1)

C-0

CHz CONH? 0 7 0 a I1 CH-C-NH-CH-C-NH-CHz-

Z-Dpr(Boc)-OH, DCC-HOBt

C.

T

I

H,-Pd

d. G-25 p a r t i t i o n c h r o m a t o g r a p h y

H-Asp-Tyr-Ile-Gln-Asn-Dpr-Pro-Leu-Gly-NH, ( 7 ) a DCC, dicyclohexylcarbodiimide; Dpr, L-a,p-diaminopropionic acid; HOBt, hydroxybenzotriazole.

mp 137-140 OC;[a]%D -48.9" (c 0.95, DMF); homogeneous on TLC (C). Anal. (CZ9HuN6O8)C, H, N. Z-A m - D p r(Boc)-Pro-Leu-Gly-NHz(2). Compound 1 (4.18 g, 6.9 mmol) was dissolved in CH30H (50 mL) and 5% Pd/C (-1 g) plus 2 drops of AcOH were added. The solution was hydrogenated for 7 h, the catalyst removed by filtration through a Celite pad, and the filtrate evaporated to dryness. The residue was dissolved in DMF (12 mL), Z-Asn-OH (1.84 g, 6.9 mmol) and HOBt (1.7 g, 11.1mmol) were added, and the solution was cooled to 0 "C. DCC (1.57 g, 7.6 mmol) was added and the solution stirred for 1h at 0 O C and 15 h at 25 "C. Dicyclohexylurea was removed by filtration and the filtrate evaporated. The residue was triturated with a small volume of HzO, filtered, and crystallized from 2-propanol: yield 4.0 g (80.6%); mp 209-211 " c ; [ a I z 5 D -36.4% (c 1.06. DMF); homogeneous on TLC (B, C). Anal. ( G ~ H ~ o N B O6, I OH,) N. Z-Gln-Asn-Dpr(Boc)-Pro-Leu-Gly-NH2 (3). The Z group was cleaved from 2 (3 g, 4.1 mmol) as described above. The free base was dissolved in DMF (9 mL), Z-Gln-OH (1.16 g, 4.1 mmol) and HOBt (1.01 g, 6.6 mmol) were added, and the solution was cooled to 0 "C. DCC (0.84 g, 4.1mmol) was added and the reaction mixture stirred a t 0 "C for 1 h and a t 25 O C for 15 h. Work-up as described above and crystallization from 95% EtOH yielded 2.5 g (72.0%) of 3: mp 188 O C ; [ a I z 5 D -45.9" (c 1, DMF); ho-

Notes

Journal of Medicinal Chemistry, 1978, Vol. 21, No. 1 119

HC1-phenol, 110 "C, 24 h): Dpr, 0.99; Asp, 1.95; Glu, 1.02; Pro, mogeneous on TLC (B). Anal. (C3BH58N10012) C, H, N. 1.00; Gly, 1.00; Ile, 0.97; Leu, 1.01; Tyr, 1.05. Z-Ile-Gln-Asn-Dpr(Boc)-Pro-Leu-Gly-NH2 (4). Compound 3 (2.5 g, 2.95 mmol) was dissolved in DMF (25 mL), Pd-black catalyst (0.5 g) added, and the reaction hydrogenated for 5 h. The Acknowledgment. The authors wish to thank Ms. S. catalyst was removed by filtration and the filtrate concentrated Chan (Chicago) for performing the bioassays and Dr. F. to 10 mL. This solution was cooled to 0 "C and Z-Ile-OH (0.86 Scheidl and his staff (Nutley) for the microanalyses, optical g, 3.24 mmol), HOBt (0.52 g, 3.4 mmol), and DCC (0.67 g, 3.2 rotations, and amino acid analysis. This work was supmmol) were added. The reaction was stirred for 1h at 0 "C and ported in part by U.S. Public Health Service Grant for 15 h a t 25 "C. After 24 h, TLC (A, B) indicated incomplete AM-18399. reaction and a further quantity of acylating agent [Z-Ile-OH (0.18 g, 0.68 mmol), HOBt (0.1 g, 0.68 mmol), and DCC (0.13 g, 0.63 References and Notes mmol)] was added after preactivation for 45 min at 0 'C in DMF. The reaction mixture was stirred for a further 24 h, dicycloAbbreviations follow generally the IUPAC-IUB Tentative hexylurea removed by filtration, and the product precipitated by Rules on Biochemical Nomenclature, J . Biol. Chem., 247, pouring the filtrate into HzO. The precipitate was filtered and 577 (1972), except Dpr, L-a,P-diaminopropionic acid. washed copiously with 1 M citric acid, H20, 1 M NaHC03, and Optically active amino acids are of the L configuration. Boc, HzO. The residue was dried and crystallized from aqueous DMF: tert-butyloxycarbonyl; But, tert-butyl; DCC, dicycloyield 1.6 g (56.5%); mp 174 "C; [o(Iz5D-41.9" (c 1, DMF); hohexylcarbodiimide; HOBt, 1-hydroxybenzotriazole; OSu, N-hydroxysuccinimide ester; Z, benzyloxycarbonyl. mogeneous on TLC (A). Anal. (CUH69N11013)c , H, N. Z-Tyr(Bu')-Ile-Gln-Asn-Dpr(Boc)-Pro-Leu-Gly-NHz (5). R. Walter, I. L. Schwartz, J. H. Darnell, and D. W. Urry, Compound 4 (1.5 g, 1.56 mmol) was hydrogenated in DMF for Proc. Natl. Acad. Sci. U.S.A., 68, 1355 (1971). 7 h as described for 4. The concentrated solution ( 5 mL) of the I. PolBEek, I. KrejEi, H. Nesvadba, and J. Rudinger, Eur. free base was cooled to 0 "C and ZTyr(But)-OH (0.64 g, 1.7 mmol), J . Pharrnacol., 9, 239 (1970). HOBt (0.38 g, 2.5 mmol), and DCC (0.35 g, 1.7 mmol) were added. R. L. Huguenin and St. Guttmann, Helv. Chim. Acta, 48, The reaction was stirred at 0 "C for 1 h and a t 25 "C for 24 h. 1885 (1965). Work-up and crystallization as described for 4 yielded 1.25g (82%) J. Rudinger and K. JoBt, Enperientia, 20, 570 (1964). of colorless crystals: mp 234-235 "C; [ o ( I z 5 ~-32.8' ( c 1, DMF); I. L. Schwartz, H. Rasmussen, and J. Rudinger, Proc. Natl. homogeneous on TLC (A, B). Anal. (C57H86N12015) C, H, N. Acad. Sci. U.S.A., 52, 1044 (1964). Z-Asp(OBut)-Tyr(But)-Ile-Gln-Asn-Dpr(Boc)-Pro-LeuK. JoBt and J. Rudinger, Collect. Czech. Chem. Commun., 32, 1229 (1967). Gly-NHz (6). Compound 5 (0.55 g, 0.466 mmol) wm hydrogenated in DMF for 14 h, as described for 4. The concentrated solution V. Pliska, J. Rudinger, T. Dousa, and J. H. Cort, Am. J. (4 mL) was cooled to 0 "C, Z-Asp(OBut)-OSu added (0.2 g, 0.48 Physiol., 215, $16 (1968). mmol), and the reaction stirred for 1 h at 0 "C and for 24 h a t K. JoBt and F. Sorm, Collect. Czech. Chem. Commun., 36, 25 "C. Work-up and crystallization as described for 4 yielded 234 (1971). 0.45 g (71.5%) of colorless crystals: mp 218-219 "C; [.Iz5D -45.8" K. JoBt,-T. Barth, I. KrejEi, L. Fruhaufovg, Z. Prochgzka, (c 0.1, DMF); homogeneous on TLC (A, B). Anal. (C%H%N13018) and F. Sorm, Collect. Czech. Chem. Commun., 38, 1073 C, H, N. (1973). [ cyclo-(1-Aspartic acid,6-a,8-diaminopropionicacid)]0. Keller and J. Rudinger, Helv. Chim. Acta, 57,1253 (1974). oxytocin (7). Compound 6 (0.2 g, 0.148 mmol) was dissolved in A. Kobayashi, S. Hase, R. Kiyoi, and S. Sakakibara, Bull. CF,COOH (5 mL) and the solution stirred for 1 h at 0 "C. After Chem. SOC. Jpn., 42, 3491 (1969). evaporation, the residual oil was triturated with ether, the triS. Sakakibara and S. Hase, Bull. Chem. SOC.Jpn., 41, 2816 fluoroacetate salt was dissolved in AcOH (3 mL) and 1.6 M (1968). S. Hase, T. Morikawa, and S. Sakakibara, Enperientia, 25, HCl-AcOH (0.4 mL), and the solution was poured into vigorously 1239 (1969). stirred anhydrous ether. The hydrochloride was filtered off and dissolved in DMF [lo mL, neutralized with NEt, (0.04 mL)], and S. Hase, S. Sakakibara, M. Wahrenburg, M. Kirchberger, a further quantity of DMF was added (90 mL). 2,2-Dipyridyl I. L. Schwartz, and R. Walter, J . Am. Chem. SOC., 94,3590 (1972). disulfide (0.12 g, 0.54 mmol) and triphenylphosphine (0.14 mg, 0.54 mmol) were added and the reaction was stirred for 72 h. The R. Walter and V. du Vigneaud, J . Am. Chem. SOC.,87,4192 solvent was evaporated, the residual yellow oil dissolved in CH30H (1965). (2 mL), and HzO (200 mL) added. The oily precipitate was R. Walter and V. du Vigneaud, J. Am. Chem. SOC.,88,1331 extracted into EtOAc (3 x 75 mL) and the combined organic (1966). phases were dried (MgS04) and evaporated. The residue was R. Walter and W. Y. Chan, J . Am. Chem. Soc., 89, 3892 reprecipitated from MeOH-EtOAc to yield 80 mg of crude (1967). N"-Z-protected oxytocin lactam. A part (45 mg) of this material C. W. Smith and M. F. Ferger, J.Med. Chem., 19,250 (1976). was dissolved in DMF (20 mL) and freshly prepared Pd-black S. Hase, S. Sakakibara, M. Wahrenburg, and R. Walter, J . (-0.1 g) added. The solution was hydrogenated for 4.5 h. The Med. Chem., 15, 1017 (1972). catalyst was removed by filtrations through a Celite pad, and the K. JoBt, A. A. Kraeviskii, and H. D. Jakubke, as cited by filtrate was evaporated to a light yellow residue (40 mg) which J. Rudinger, Proc. R. Soc., Ser. B, 170, 17 (1968). was chromatographed on a 2.5 x 100 cm column of Sephadex G-25 W. Konig and R. Geiger, Chem. Ber., 103, 788 (1970). and eluted with 0.2 M AcOH. Fractions (5 mL) containing the T. Mukaiyama, R. Matsueda, and H. Maruyama, Bull. major product with minor impurities were pooled and lyophilized Chem. SOC.Jpn., 43, 1271 (1970). to yield 34 mg of a colorless powder. This was further subjected D. Yamashiro, Nature (London), 201, 76 (1964); D. Yato partition chromatographyz4 on a 2.2 X 52 cm column of mashiro, D. Gillessen, and V. du Vigneaud, J . Am. Chem. Sephadex G-25 (100-200 mesh block polymerizate) in the system Soc., 88, 1310 (1966). 1-BuOH-HzO containing 3.5% AcOH and 1.5% pyridine (1:1, P. Holton, Br. J. Pharmacol. Chemother., 3,328 (1948); R. v/v). The column, which had been equilibrated with both phases A. Munsick, Endocrinology, 66, 451 (1960). of the solvent system, was eluted with upper phase at 12-16 mL/h J. M. Coon, Arch. Int. Pharmacodyn. Ther., 62,79 (1939); into 3.2-mL fractions. Peptide material was detected by the "The Pharmacopeia of the United States of America", 18th method of Lowry et al.= The product emerged as a symmetrical revision, Mack Publishing Co., Easton, Pa., 1970, p 469; R. peak with a maximum at Rf 0.16; fractions corresponding to the A. Munsick, W. H. Sawyer, and H. B. Van Dyke, Endopeak area (86-100) were pooled and the product was isolated by crinology, 66, 860 (1960). -106' (c 0.5, 1 N AcOH). TLC lyophilization: wt 16.0 mg; [cx]~D "The Pharmacopeia of the United States of America", 18th showed the product as a single spot, R, 0.24 (BuOH-AcOH-HzO, revision, Mack Publishing Co., Easton, Pa., 1970, p 771. 4:1:1), R10.53 (BuOH-pyridine-AcOH-HzO, 15:10:3:6), in loads W. A. Jeffers, M. M. Livezey, and J. H. Austin, Proc. SOC. up to 50 bg developed for 120 mm. Anal. (C.&67N13013J.X3Enp. Bid. Med., 50, 184 (1942). COOH.H20) (986.1 + 78.1) C, H, N. Amino acid analysis36 (6 N W. H. Sawyer, Endocrinology, 63, 694 (1958).

120 Journal of Medicinal Chemistry, 1978, Vol. 21, No. I

(30) H. 0. Schild, J. Physiol. (London), 101, 115 (1942). (31) J. Meienhofer, J . Am. Chem. SOC., 92, 3771 (1970). (32) S. Moore, R. P. Patel, E. Atherton, M. Kondo, J. Meienhofer, L. Blau, R. Bittman, and R. K. Johnson, J . Med. Chem., 19, 766 (1976). (33) Prepared from Boc-Pro-Leu-Gly-NH2 (ref 34) by treatment with 2 M HCl in tetrahydrofuran for 1 h a t room temperature: mp 181-184 "C; [a]25D-50.6" (c 0.1,O.l M HCl).

Notes Anal. (C13H25N403C1) C1. (34) T. Mizoguchi, K. Shigezane, and N. Takamura, Chem. Pharm. Bull., 18,1465 (1970); A. S. Duta and J. S. Morley, J . Chem. SOC. C, 2896 (1971). (35) 0. H. Lowry, N. J. Rosebrough, A. L. Farr, and R. J. Randall, J . Biol. Chem., 193, 265 (1951). (36) D. H. Spackman, W. H. Stein, and S. Moore, Anal. Chem., 30, 1190 (1958).

Inhibitory Analogues of the Luteinizing Hormone-Releasing Hormone Having D-Aromatic Residues in Positions 2 and 6 and Variation in Position 3l John Humphries, Yieh-Ping Wan, Karl Folkers,* Institute for Biomedical Research, University of Teras a t Austin, Austin, Texas 78712

and Cyril Y. Bowers Tulane University, New Orleans, Louisiana 70112. Received May 27, 1977 A single sc injection of 750 pg/rat of [ D - P ~ ~ ~ , P ~ O ~ , D - P ~ ~on ' ] proestrus - L H - R Hcompletely inhibited ovulation in 4-day cycling rats. Ovulation was inhibited partially at 375 ,ug/rat. At the 750 pg/rat dosage, analogues of LH-RH with D-Phe in positions 2 and 6, and with Sar, Arg, or Hyp in position 3, resulted in partial inhibitors and an inactive analogue with Thr substitution. In the same assay, analogues with D-Phe in position 2 and D-Trp in position 6 were partial inhibitors when D-Phe, Met, or Val were in position 3 and inactive with Ile substitution.

Since our report that a disubstituted LH-RH analogue, [Leu2,Leu3]-LH-RH,could inhibit the action of LH-RH in an in vitro assay using isolated whole rat pituitaries,2 we have synthesized more analogues based on this seq ~ e n c e . "Of ~ special interest was the design of an LH-RH inhibiting peptide that could effectively suppress ovulation. The observations by Corbin and c o - ~ o r k e r sthat , ~ [DPhe2,~-Ala6]-LH-RH could inhibit ovulation in rats and rabbits and prevent pregnancy when appropriately administered, precoitally, a t a dosage of 24 mg/ kg sc, have stimulated the synthesis of analogues of LH-RH having a D-Phe residue in position 2. It was also realized that the incorporation of a D-amino acid residue in position 6, which followed from some of the work of Monahan et a1.,6 was seemingly essential for high antiovulatory activity in rats. However, when the modification of Fujino et al.7 was applied to the [D-Phe2,D-Ala6]-LH-RHsequence, the resulting des-Gly'O- [ D - P ~ ~ ' , D - A ~ ~ ~ ] - Lethylamide H - R H was found to be a superior inhibitor of LH-RH action, in vitro, using a monolayer technique but did not inhibit ovulation.* Recently, Humphries et aln9reported that [D-Phe2,Pro3,~-Trp6]-LH-RH inhibited the release of LH and FSH by LH-RH, in vitro, a t a ratio of ana1ogue:LH-RH of 50:l. This analogue also completely inhibited ovulation in 4-day cycling rats a t a single sc injection of 750 pg, and partial inhibition of ovulation was also observed a t a 375-pg dosage. The analogues, [D-Phe2,Leu3,~-Trp6]-LH-RH and [ D - P ~ ~ ~ , L ~ U ~ , D - P ~were ~ ~ ]less -LH effective. - R H Bowers and Folkers'O have shown that the infusion into rats of [ D - P ~ ~ ~ , P ~ ~ ~ , D - T ~ from ~ ~ ] Ia -sc LH implanted, - R H , osmotically driven minipump, a t a rate of 375 pg/day for 4 days, completely inhibited ovulation in 4-day cycling rats. This paper describes the synthesis and activities of some further analogues of LH-RH, having a D-Phe residue in position 2, amino acid substitution in position 3, and a D-aromatic amino acid in position 6, in a continuing effort to evaluate structure-activity relationships for inhibition of ovulation.

Experimental Section The procedure of solid-phase peptide synthesis was essentially identical with that d e ~ c r i b e d . ~Amino acid derivatives were 0022-2623/78/1821-0120$01.00/0

supplied by Peninsula Laboratories, Beckman Bioproducts Division, or Sigma. Product yields (%) were estimated from the starting amino acid-resin. On chromatography, the product of the major peaks was examined by TLC. Usually only those fractions corresponding to the upper parts of the peak were taken, and consequently the percentage yields will be low. Completed, protected peptide-BHA resins were cleaved and deblocked by reaction for 1 h at 0 "C with CoF3-dried liquid HF" containing ca. 20% anisole. TLC on silica gel was used to evaluate product purity, with the systems Rf', EtOAc-H20-AcOH-1-Bu0H (1:l:l:l v/v); Rf2, EtOAc-pyridine-AcOH-H20 (5:5:1:3 v/v); RQ, propan-2-01-1 N AcOH (2:l v/v); and R t , 0.1% AcOH-1-BuOH-pyridine (11:5:3 vjv, upper phase). Peptide spots were negative to ninhydrin and positive to chlorine-0-tolidine reagent. Amino acid analyses, on ca. 0.5-mg samples hydrolyzed in 6 N HCl in evacuated and sealed ampules for 18 h at 110 "C, were performed using a single column methodology on a Beckman Model 119 amino acid analyzer equipped with an Infotronics Model CRS-210 automatic digital integrator. Optical rotations were measured on a Perkin-Elmer 141 digital read-out polarimeter. Synthesis of the 3-Substituted [ ~ - p h e ~ , ~ - p h e ~ ] - L H - R H Analogues. Benzhydrylamine (BHA)-resin hydrochloride (10 g, 0.44 mequiv/g, Beckman Bioproducts) was sized in CH2C12, neutralized, and coupled with Boc-Gly. The Boc-Gly-BHA resin was submitted to six cycles of deprotection, neutralization, and coupling to yield the heptapeptide BHA-resin, Boc-Ser(Bz1)Tyr(BrZ)-D-Phe-Leu-Arg(Tos)-Pro-Gly-BHA resin (15.38 g). Two-gram portions of the heptapeptide BHA-resin were submitted to further coupling cycles, with the appropriate position 3 amino acid derivative, then Boc-D-Phe, and finally Z-